Beta-diketones substituted by an aryl-aliphatic group in which the aliphatic chain is interrupted by a cyclic group, and useful as anti-viral agents, are prepared by interacting the appropriate aryl-aliphatic halide with an alkali metal salt of a beta-diketone.
通过将适当的芳基-脂肪基卤化物与
β-二酮的碱
金属盐相互作用,制备了由芳基-脂肪基替代的
β-二酮,其中脂肪链被一个环状基团中断,并且这些化合物可用作抗病毒剂。